Tag | Content |
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EnhancerAtlas ID | HS101-03716 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:204560610-204561730 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:204561216-204561234 | GGAATGAATGAAGCAAAG | + | 6.24 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 204560899 | 204561181 | chr1 | 204561583 | 204561691 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I204591 | chr1 | 204560516 | 204561648 |
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Enhancer Sequence | GACAAGCTGA TCTCCAATTT TCTAATCTTT AAAATGGGCT GGGAGAGTGT TGTGATGATG 60 AAATGAACTA ATACAGTAAA GTGCCTGGCA TATAGCTGGT GCCCAAGCAG CTCCTTCTGC 120 AGGAAGCCTT CCCTGACTTC TCCAGACCTG GTCAGGTACC TTCATTTCCA CACACCAGCC 180 TTGATGCATG TGTCATTCAA AGCCGTGTGT CAACAACAGT GCAGATCTTT GACAGTCACA 240 GACCTTTGTG GGTATTTACT GAATAGTCAA ACGGCAAATA TGGAATCTGC AAATGCCAAG 300 AGCCTACTAT ATTGGAACAT TTTTATCTTT CTGGTCCCTA CTCTCTCCTA GGCTTTCAGA 360 TCTTGAGGGT ACAACGTGGT TATTTCTCAG CTTTGCTTCT CCCCAGCTGT CAAAAGTGCT 420 CAATAAATAT TTGACCACTG AGTAACTTTT AAGTTACTCA TGCATGAGTA ATTGAATAAA 480 TGCATGAAAG AATGCATACA CTAGTGAATG TATGAATAAT AGAATGAGAC AATTAGTGCA 540 TAAGTGGGGG AAATAGGTGA ATGGTGAATC AAGAAATGAG TAGAGAATTA AAGGAGTGAA 600 GGTGAAGGAA TGAATGAAGC AAAGCTGGTT ACCTTTCTTC CAAAGGGCTA TGTGCTGGTG 660 ACAATACAAA TGGGCCCATT CCAGAGCCCT GGAGAGAGTT AGAGCTGGTC CACCTGACAG 720 ACAGCCACGA GTGACAGCCC AGCCACTGGG GTCCTCCAAA TGTACTCATT CTGGAAACTT 780 CTCCTTTCCT TCCAGCCACT ATCTGCCACC CCTCCATGGA GCTAGGGACG CCAAGGGACT 840 GTGAGGCAGG GCATGACTCC AGGGGGCAGA GAGCTAAGTG CATGGCTGTC CTCTCTCTTC 900 CCAAACCCTT GTCACAGGCC GTGAGGGCCT GCTGCCTCCC CTGATGCCAT GTTCCTGAGC 960 AGATGTTCCT CCTGTCTTGT CAGCAACAGA GCGGCTGTCA GGAGTCCGCA TTATATATCT 1020 GCTCGGTAAC GTTTACTGGG ATTTAGTGTT TAACAACTGT CACTCCAATA TATCTTTTCT 1080 TAATCCCTTC AGATCTGCTG CTGTAGCAAC TTTAAATATT 1120
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